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GABA‐Related phenomena, models of nervous system function, and seizures
Author(s) -
Roberts Eugene
Publication year - 1984
Publication title -
annals of neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.764
H-Index - 296
eISSN - 1531-8249
pISSN - 0364-5134
DOI - 10.1002/ana.410160713
Subject(s) - neuroscience , gabaergic , inhibitory postsynaptic potential , thalamic reticular nucleus , reticular activating system , central nervous system , disinhibition , nervous system , biological neural network , biology , thalamus , excitatory postsynaptic potential , reticular formation
Models of nervous system function are presented that place particular emphasis on the roles in nervous system function of inhibitory neurons that liberate γ‐aminobutyric acid (GABA) as neurotransmitter. The nervous system is considered to be highly restrained, with inhibitory neurons acting like reins that serve to keep the neuronal “horses” from running away. In behavioral sequences, whether innate or learned, preprogrammed circuits are released to function at varying rates and in various combinations. This release is accomplished largely by the disinhibition of pacemaker neurons whose activities are under the control of tonically active inhibitory command neurons, many of which may use GABA as a transmitter. In addition to their restraining function, local circuit GABA ergic neurons participate in feed‐forward, feedback, surround, and presynaptic inhibition and inpresynaptic facilitation. Information arriving from several sources is integrated in specialized analyzing regions, such as the cerebellar cortex, basal ganglia, and reticular nucleus of the thalamus. Monosynaptic inhibitory GABA ergic output reflecting this analysis then play upon neural elements in the direct channels, making their activity optimally compatible temporally and spatially with that of neural elements elsewhere in the central nervous system. Seizures are prototypical of incoordination between inhibition and excitation. Major causes of seizures may be the loss of inhibitory GABA ergic terminals at the site of focal cortical epilepsy or a disturbance in various aspects of GABA ergic function.